chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109794098397940984C12GENIChomozygous128850840
109794098997940990A12GENIChomozygous128850841
109794099397940994C13GENIChomozygous128850842
109794099497940995CT13GENIChomozygous116907048
109794099897940999C14GENIChomozygous128850843
109794100297941003A14GENIChomozygous128850844
109794100497941006CT14GENIChomozygous128850845
109794107797941077C19GENIChomozygous128850846
109794116097941160C19GENIChomozygous128850847
109794119797941197C14GENIChomozygous128850848
109794122697941227C11GENIChomozygous128850849
109794123197941232C11GENIChomozygous128850850
109794125597941256C9GENIChomozygous128850851
109794131197941311CGCC20GENIChomozygous128850852
109794144497941444CC20GENIChomozygous128850856
109794131797941318A18GENIChomozygous128850853
109794141897941419C15GENIChomozygous128850854
109794143897941438G19GENIChomozygous128850855
109794146097941461C21GENIChomozygous128850857
109794164297941643TC30GENIChomozygous116695392
109794485297944853AG21GENIChomozygous116695400
109794675697946757CT16GENIChomozygous116695402
109794768597947686AG16GENIChomozygous116695406
109794909697949097TG20GENIChomozygous116695408
109794943697949437T23GENICpossibly homozygous133233351
109794281597942827GTGTGTGTGTGC18GENIChomozygous133233349
109794691697946917C17GENIChomozygous133233350
109794289697942897TC10GENIChomozygous117023938
109794703197947032CT36GENIChomozygous117023942
109795035597950356CA24GENIChomozygous116695410
109795068497950685CT23GENIChomozygous117023944
109795141297951413AG12GENIChomozygous116695412
109795166297951663AC15GENIChomozygous116695414
109795281497952815TC26GENIChomozygous116695416
109795389197953892GT18GENIChomozygous116695418
109795610997956110CT23GENIChomozygous117023945
109795791797957918GA19GENIChomozygous117414185
109795793797957938GA23GENIChomozygous117023947
109795814597958145T17GENIChomozygous133233352
109795883397958834CT19GENIChomozygous117372700
109795885297958853GC18GENIChomozygous116695426